| 國立成功大學 |
2023 |
Changing clinical manifestations of Gaucher disease in Taiwan
|
Lu, W.-L.;Chien, Y.-H.;Tsai, F.-J.;Hwu, W.-L.;Chou, Y.-Y.;Chu, S.-Y.;Li, M.-J.;Lee, A.-J.;Liao, C.-C.;Wang, C.-H.;Lee, N.-C. |
| 國立成功大學 |
2023 |
Combining Panel-Based Next-Generation Sequencing and Exome Sequencing for Genetic Liver Diseases
|
Chen, Chen C.-B.;Hsu, J.S.;Chen, P.-L.;Wu, J.-F.;Li, H.-Y.;Liou, B.-Y.;Chang, M.-H.;Ni, Y.-H.;Hwu, W.-L.;Chien, Y.-H.;Chou, Y.-Y.;Yang, Yang Y.-J.;Lee, N.-C.;Chen, H.-L. |
| 國立成功大學 |
2023 |
Harnessing polyhydroxylated pyrrolidines as a stabilizer of acid alpha-glucosidase (GAA) to enhance the efficacy of enzyme replacement therapy in Pompe disease
|
Li, H.-Y.;Lee, N.-C.;Chiu, Y.-T.;Chang, Y.-W.;Lin, C.-C.;Chou, Chou C.-L.;Chien, Y.-H.;Hwu, W.-L.;Cheng, W.-C. |
| 臺大學術典藏 |
2022-09-15T05:47:52Z |
Vohwinkel syndrome associated with a p.Gly59Arg missense mutation in GJB2
|
Hsieh P.-C.; Chen-Chi Wu; Lee N.-C.; Hsieh J.-H.; Liao Y.-H. |
| 臺大學術典藏 |
2022-09-15T02:48:40Z |
A case of GNE myopathy mimicking hereditary motor neuropathy
|
Huang, Y-N; Chuang, H-J; Hsueh, H-W; HSIN-CHIEH HUANG; Lee, N-C; Chao, C-C; HUANG, P-H; Lee, Y-C; Lin, K-P; Yang, C-C; Hsieh, S-T |
| 臺大學術典藏 |
2022-09-15T02:44:08Z |
A case of senile-onset progressive hemiballism and cognitive decline with diffuse brain iron accumulations
|
Lin I.-T.; Lee N.-C.; Fan S.-P.; Huang C.-J.; Cheng P.; Chen J.-H.; CHIN-HSIEN LIN |
| 臺大學術典藏 |
2022-09-06T02:56:09Z |
Duchenne muscular dystrophy newborn screening: the first 50,000 newborns screened in Taiwan
|
YIN-HSIU CHIEN; Lee N.-C.; Weng W.-C.; Chen L.-C.; Huang Y.-H.; Wu C.-S.; Hwu W.-L. |
| 臺大學術典藏 |
2022-09-06T02:56:09Z |
Safety and efficacy of eliglustat combined to enzyme replacement therapy for lymphadenopathy in patients with Gaucher disease type 3
|
Lee N.-C.; YIN-HSIU CHIEN; Wang C.-H.; Wong S.-L.; Peng S.S.-F.; Tsai F.-J.; Hwu W.-L. |
| 臺大學術典藏 |
2022-09-06T02:56:07Z |
Improved diagnosis of citrin deficiency by newborn screening using a molecular second-tier test
|
Chen H.-A.; Hsu R.-H.; Chen Y.-H.; Hsu L.-W.; Chiang S.-C.; Lee N.-C.; Hwu W.-L.; Chiu P.-C.; YIN-HSIU CHIEN |
| 臺大學術典藏 |
2022-09-06T02:56:07Z |
High incidence of null variants identified from newborn screening of X-linked adrenoleukodystrophy in Taiwan
|
Chen H.-A.; Hsu R.-H.; Chen P.-W.; Lee N.-C.; Chiu P.-C.; Hwu W.-L.; YIN-HSIU CHIEN |
| 臺大學術典藏 |
2022-09-06T02:56:06Z |
Comparison of GATK and DeepVariant by trio sequencing
|
Lin Y.-L.; Chang P.-C.; Hsu C.; Hung M.-Z.; YIN-HSIU CHIEN; Hwu W.-L.; Lai F.P.; Lee N.-C. |
| 臺大學術典藏 |
2022-03-28T06:27:48Z |
CTLA-4 gene mutation and multiple sclerosis: A case report and literature review
|
Lin T.-W.; Hu Y.-C.; YAO-HSU YANG; Chien Y.-H.; Lee N.-C.; Yu H.-H.; Chiang B.-L.; Wang L.-C. |
| 臺大學術典藏 |
2022-03-28T02:46:03Z |
Hypothermia improves disease manifestations in SMA mice via SMN augmentation
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Tsai L.-K.; Chen C.-L.; Tsai Y.-C.; Ting C.-H.; YIN-HSIU CHIEN; Lee N.-C.; Hwu W.-L. |
| 臺大學術典藏 |
2022-03-28T02:46:02Z |
CTLA-4 gene mutation and multiple sclerosis: A case report and literature review
|
Lin T.-W.; Hu Y.-C.; Yang Y.-H.; YIN-HSIU CHIEN; Lee N.-C.; Yu H.-H.; Chiang B.-L.; Wang L.-C. |
| 臺大學術典藏 |
2022-03-28T02:46:00Z |
Rapid Trio Exome Sequencing for Autosomal Recessive Renal Tubular Dysgenesis in Recurrent Oligohydramnios
|
Lin S.-Y.; Chuang G.-T.; Hung C.-H.; Lin W.-C.; Jeng Y.-M.; Yen T.-A.; Chang K.; YIN-HSIU CHIEN; Hwu W.-L.; Lee C.-N.; Tsai I.-J.; Lee N.-C. |
| 臺大學術典藏 |
2022-03-28T02:45:58Z |
RNA-seq of peripheral blood mononuclear cells of congenital generalized lipodystrophy type 2 patients
|
Huang Y.-H.; Su T.-C.; Wang C.-H.; Wong S.-L.; YIN-HSIU CHIEN; Wang Y.-T.; Hwu W.-L.; Lee N.-C. |
| 臺大學術典藏 |
2022-03-28T02:45:58Z |
A pilot study shows the positive effects of continuous airway pressure for treating hypernasal speech in children with infantile-onset Pompe disease
|
Zeng Y.-T.; Liu W.-Y.; Torng P.-C.; Hwu W.-L.; Lee N.-C.; Lin C.-Y.; YIN-HSIU CHIEN |
| 臺大學術典藏 |
2022-03-28T02:45:57Z |
A novel deep intronic variant strongly associates with Alkaptonuria
|
Lai C.-Y.; Tsai I.-J.; Chiu P.-C.; Ascher D.B.; YIN-HSIU CHIEN; Huang Y.-H.; Lin Y.-L.; Hwu W.-L.; Lee N.-C. |
| 臺大學術典藏 |
2022-03-28T02:45:54Z |
Novel compound heterozygous variants in tbcd gene associated with infantile neurodegenerative encephalopathy
|
Chen C.-L.; Lee C.-N.; YIN-HSIU CHIEN; Hwu W.-L.; Chang T.-M.; Lee N.-C. |
| 臺大學術典藏 |
2022-03-28T02:45:53Z |
Outcome of Later-Onset Pompe Disease Identified Through Newborn Screening
|
Lee N.-C.; Chang K.-L.; in 't Groen S.L.M.; de Faria D.O.S.; Huang H.-J.; Pijnappel W.W.M.P.; Hwu W.-L.; YIN-HSIU CHIEN |
| 臺大學術典藏 |
2022-03-28T02:45:53Z |
Short stature leads to a diagnosis of Jansen–de Vries syndrome in two unrelated Taiwanese girls: A case report and literature review
|
Tsai M.-J.M.; Lee N.-C.; YIN-HSIU CHIEN; Hwu W.-L.; Tung Y.-C. |
| 臺大學術典藏 |
2022-03-28T02:45:46Z |
Long-term efficacy and safety of eladocagene exuparvovec in patients with AADC deficiency
|
Tai C.-H.; Lee N.-C.; YIN-HSIU CHIEN; Byrne B.J.; Muramatsu S.-I.; Tseng S.-H.; Hwu W.-L. |
| 臺大學術典藏 |
2022-03-17T02:52:54Z |
UNC13D mutation presenting as fulminant familial hemophagocytic lymphohistiocytosis
|
Liao C.-H.; Lee N.-C.; Jou S.-T.; Chiang B.-L.; HSIN-HUI YU |
| 臺大學術典藏 |
2022-03-17T02:52:54Z |
CTLA-4 gene mutation and multiple sclerosis: A case report and literature review
|
Lin T.-W.; Hu Y.-C.; Yang Y.-H.; Chien Y.-H.; Lee N.-C.; HSIN-HUI YU; Chiang B.-L.; Wang L.-C. |
| 臺大學術典藏 |
2022-03-10T02:31:41Z |
Novel heterozygous tissue-nonspecific alkaline phosphatase (TNAP) gene mutations causing lethal perinatal hypophosphatasia
|
Chang K.-C.; PO-HAN LIN; Su Y.-N.; Peng S.S.-F.; Lee N.-C.; Chou H.-C.; Chen C.-Y.; Hsieh W.-S.; Tsao P.-N. |
